Actively Recruiting

Age: 18Years +
All Genders
ID07311941

Rapid Escalation of Lipid Lowering Therapy to Reduce Recurrent Cardiovascular Event (REDUCE) All Comers Study

Led by Chinese University of Hong Kong · Updated on 2025-12-31

1000

Participants Needed

1

Research Sites

25 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This research aims to evaluate the impact of frequent monitoring and adjustment of lipid-lowering therapy (LLT) to achieve target low-density lipoprotein cholesterol (LDL-C) levels in patients with hyperlipidemia and cardiovascular disease. The study focuses on patients with acute or chronic coronary syndrome due to atherosclerotic coronary artery disease. Despite guidelines recommending aggressive LDL-C lowering primarily with statins, many patients do not reach their LDL-C goals due to factors like non-adherence and limited use of additional therapies. Participants include patients diagnosed with acute or chronic coronary syndrome caused by atherosclerosis. The study observes how frequent LDL-C testing and timely changes in LLT at a specialist clinic affect LDL-C control. There is no interventional treatment assigned; rather, the study collects data on LDL-C levels and therapy adjustments over time to assess current clinical practice strategies. During the study, LDL-C levels will be measured at baseline and at weeks 8, 26, and 52. Researchers will also monitor participants' achievement of LDL-C targets, adherence to lipid-lowering therapy, tolerability, and any major cardiovascular events. Quality of life will be assessed using the 12-Item Short Form Survey at the same time points. The study is observational, with follow-up lasting up to one year to gather comprehensive data on lipid management and cardiovascular outcomes.

CONDITIONS

Brief Title

Rapid Escalation of LipiD Lowering Therapy to Reduce RecUrrent Cardiovascular Event

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age over 18 years
  • Diagnosis of acute coronary syndrome due to atherosclerotic coronary artery disease
  • Diagnosis of chronic coronary syndrome due to atherosclerotic coronary artery disease
Not Eligible

You will not qualify if you...

  • Unable to provide valid consent by the patient or legal guardian
  • Acute coronary syndrome due to causes other than atherosclerotic coronary artery disease
  • Psychiatric or severe neurological disorder, cirrhosis, or active malignancy with life expectancy less than 6 months

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Monitoring

Duration - 52 weeks

Participants are monitored over time with regular assessments of cholesterol levels and cardiovascular health.

Visits at Baseline, Week 8, Week 26, and Week 52

Trial Site Locations

Total: 1 location

1

Prince of Wales Hospital

Shatin, New Terrritories, Hong Kong, 999077

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Research Team

G

Guangming Tan

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

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